Fedota John R, Sutherland Matthew T, Salmeron Betty Jo, Ross Thomas J, Hong L Elliot, Stein Elliot A
Neuroimaging Research Branch, National Institute on Drug Abuse, Intramural Research Program, National Institutes of Health, Baltimore, MD, USA.
Department of Psychology, Florida International University, Miami, FL, USA.
Neuropsychopharmacology. 2015 Jul;40(8):2038-46. doi: 10.1038/npp.2015.54. Epub 2015 Mar 6.
Recidivism rates for cigarette smokers following treatment often exceed 80%. Varenicline is the most efficacious pharmacotherapy currently available with cessation rates of 25-35% following a year of treatment. Although the in vivo binding properties are well known, varenicline's neurobiological mechanisms of action are still poorly understood. Varenicline acts as a nicotinic receptor partial agonist or antagonist depending on the presence or absence of nicotine and has been implicated in the reduction of reward signaling more broadly. The current study probed anticipatory reward processing using a revised monetary incentive delay task during fMRI in cohorts of smokers and non-smokers who completed a two-drug, placebo-controlled, double-blind crossover study. All participants underwent ~17 days of order-balanced varenicline and placebo pill administration and were scanned under each condition wearing a transdermal nicotine or placebo patch. Consistent with nicotine's ability to enhance the rewarding properties of nondrug stimuli, acute nicotine administration enhanced activation in response to reward-predicting monetary cues in both smokers and non-smokers. In contrast, varenicline reduced gain magnitude processing, but did so only in smokers. These results suggest that varenicline's downregulation of anticipatory reward processing in smokers, in addition to its previously demonstrated reduction in the negative affect associated with withdrawal, independently and additively alter distinct brain circuits. These effects likely contribute to varenicline's efficacy as a pharmacotherapy for smoking cessation.
接受治疗后的吸烟者复发率通常超过80%。伐尼克兰是目前最有效的药物疗法,经过一年治疗后戒烟率为25%-35%。尽管其体内结合特性已为人所知,但伐尼克兰的神经生物学作用机制仍知之甚少。根据是否存在尼古丁,伐尼克兰可作为烟碱受体部分激动剂或拮抗剂,并且更广泛地参与减少奖赏信号。本研究在功能磁共振成像(fMRI)期间,使用修订后的金钱激励延迟任务,对完成两药、安慰剂对照、双盲交叉研究的吸烟者和非吸烟者队列进行预期奖赏加工探究。所有参与者接受了约17天的伐尼克兰和安慰剂药丸顺序平衡给药,并在每种条件下佩戴透皮尼古丁或安慰剂贴片进行扫描。与尼古丁增强非药物刺激奖赏特性的能力一致,急性尼古丁给药增强了吸烟者和非吸烟者对奖赏预测金钱线索的激活反应。相比之下,伐尼克兰降低了增益幅度加工,但仅在吸烟者中如此。这些结果表明,伐尼克兰除了先前证明的减少与戒断相关的负面影响外,还下调吸烟者的预期奖赏加工,独立且累加地改变不同的脑回路。这些效应可能有助于伐尼克兰作为戒烟药物疗法的疗效。